NBME9 Flashcards

1
Q

34-year-old F presents to the ED 1 hour after an episode of palpitations, sweating, and shortness of breath. The episode occurred while she was at her job. She thought that she was having a heart attack. She reports she has been under increased stress at work. This is her fourth visit to the emergency department during the past 3 weeks for similar symptoms. At each prior visit, workup and physical exam was normal.
Today her vitals are:
HR 88
RR: 16
BP 128/70
PE unremarkable. Labs normal including cardiac workup. An ECG shows sinus arrhythmia.
MSE: tense and fearful. linear thought process, no hallucination or delusions.

What is the most likely diagnosis?
A. Myocardial infarction
B. Cocaine intoxication
C. PTSD
D. Acute stress disorder
E. Panic disorder
F. Unstable angina pectoris

A

Panic disorder

Panic attacks feature acute fear or anxiety that peaks within minutes and are associated with four additional physical symptoms (eg, diaphoresis, chest pain, dyspnea) or associated mental states secondary to sympathetic overactivation. Panic disorder is an anxiety disorder characterized by recurrent panic attacks that are unexpected and associated with worry about future panic attacks or avoidance of panic attack triggers.

Per DSM V, panic attacks must be present for ≥1 month
Tx: CBT, SSRI (venlafaxine), benzo for acute

Acute stress disorder ≤1 month of symptoms after known stressful event

PTSD >1 month of symptoms, avoidance of triggers, known traumatic event (work stress doesn’t count)

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2
Q

A 23-year-old woman, gravida 1, para 1, comes to the office in January for a follow-up examination 6 weeks after term NSVD of her son. Pregnancy and delivery were uncomplicated. She says she has been tearful during the past 3 weeks and has not left the house since visiting relatives 2 weeks ago. She says she loves her son and husband, but she has not enjoyed spending time with them during the past 2 weeks. She wakes up every 3 hours at night to breast-feed her infant and is unable to sleep well even when her husband offers to care for their son. She spends most of the day in bed with her infant in a crib nearby; she gets up only to feed and change him. She has no history of serious illness, takes no medications, and has no known allergies. Physical examination shows no abnormalities. On mental status examination, she has a depressed mood and flat affect. She does not have suicidal or homicidal ideation. She has not had audio or visual hallucinations. Which of the following is the most likely diagnosis?
A. Bipolar disorder
B. Major depressive disorder
C. Postpartum psychosis
D. Seasonal affective disorder
E. Normal postpartum course

A

MDD
This patient demonstrates depressed mood, anhedonia (decreased enjoyment of socializing), and insomnia along with decreased social functioning (not spending time with her husband or baby outside of tending to her baby’s basic needs), making an major depressive disorder diagnosis likely.

Symptoms of major depressive disorder include ≥2 weeks of ≥5 of the following symptoms:
-depressed mood*
-anhedonia
-guilt or worthlessness
-difficulty concentrating
-psychomotor retardation or agitation
-suicidal thoughts
-neurovegetative symptoms (decreased energy, sleep disturbance, appetite disturbance)

postpartum blues can be part of a normal postpartum course but resolved within 2 weeks of delivery.

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3
Q

What is the illness script for delirium tremens?

What electrolyte abnormalities could you expect to find?

A

Alcoholic w/ 48 hours-1 week after last drink w/ presenting symptoms of:
-severe confusion and disorientation
-fluctuations in consciousness
-agitation
-visual or auditory hallucinations
- autonomic instability (fluctuations in HR and BP with hyperthermia).
Managed w/ benzodiazepines (eg, lorazepam) to address agitation and prevent the symptoms of withdrawal, along with fluids, nutritional supplementation of deficient vitamins and minerals, and frequent assessment including vital sign checks.

The vitamins that are commonly deficient in patients with alcohol use disorder include thiamine, folate, vitamin B , vitamin A, and vitamin B, and mineral deficiency of
magnesium, iron, and zinc.

The pathogenesis of hypomagnesemia is likely related to decreased oral intake and alcohol induced urinary excretion of magnesium.

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4
Q

what study metric incorporates morbidity and mortality into one?

A

DALY (disability-adjusted life years) is a metric of overall disease burden that takes into account years of life lost caused by death AND years of healthy life lost as a result of disability

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5
Q

what is a potential source of bias in retrospective studies like case-control studies that depend on reported data from participants as opposed to chart review?

A

Recall bias occurs when participants do not remember or omit details or experiences related to previous or related events. It is a potential source of bias in retrospective studies, especially those in which the exposure may have occurred many years ago, which is common when diseases under study have long latency periods.

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6
Q

How do you calculate the NNT from absolute risks of two groups?

A

ARR= RR control- RR intervention (in decimal form)
ie if RR control= 15% and RR intervention=13%, then
ARR=0.15-0.13=0.02

NNT=1/ARR = 1/0.02=50 in this example

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7
Q

Define attributable risk and how to calculate it

A

Attributable (excess) risk (AR) describes the risk of developing disease or the outcome under study that can be attributed to the exposure as compared to the risk that exists without the exposure.
AR= (incidence of exposed group) - (incidence of non exposed group)

AR = (a / (a + b)) - (c / (c + d))
a= exposed and have disease
b= exposed and don’t have disease
c= not exposed and don’t have disease
d= not exposed and have disease

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8
Q

Define relative risk and how to calculate it. What studies use RR? What about RRR?

A

Relative risk (RR) describes the difference in likelihood of the occurrence of a particular disease outcome between two groups of patients with or without a particular exposure.
Calculations of RR are commonly performed in cohort studies.

RR = (a / (a + b)) / (c / (c + d))
RR= (incidence of exposed) / (incidence of nonexposed)

RR values greater than 1.0 indicate an increased risk of developing disease in association with the exposure, whereas values less than 1.0 indicate a reduced risk of developing disease, and RR equal to 1.0 indicates that the disease outcome and the exposure are not associated in any particular direction.

Relative Risk Reduction= 1-RR

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9
Q

What cell type is most likely to be increased in a patient w/ bone pain, anemia, hypercalcemia, kidney dysfunction, and lytic bone lesions who is found to have a monoclonal gammopathy on protein electrophoresis?

A

Monoclonal B lymphocyte

Signs and symptoms of MM include bone pain, anemia, hypercalcemia, kidney dysfunction, and lytic bone lesions. B-lymphocytes are precursors to plasma cells, which secrete specific immunoglobulins of different classes and are considered terminally differentiated B-lymphocytes.
**MM is a malignancy caused by the neoplastic proliferation of a single plasma cell clone, which overproduces monoclonal immunoglobulin and light or heavy chains. These clonal immunoglobulins are secreted in high numbers and appear as a monoclonal spike on protein electrophoresis in the gamma region on protein electrophoresis. Diagnosis of multiple myeloma is suspected based on the presence of an M-protein spike in the presence of concerning symptoms, but is confirmed by bone marrow biopsy, which must demonstrate at least 10% clonal plasma cells.

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10
Q

A 67-year-old man w/ long history of poorly controlled HTN presenting w/ 1 hour after the onset of vertigo, nausea, and imbalance.
Vitals: pulse 70/min, respirations 20/min, and blood pressure 210/115 mm Hg.

Physical examination:
small left pupil, mild left ptosis, and nystagmus.
Neurologic examination: weakness of the left palate; Sensation to pinprick is decreased over the left side of the face and right extremities. Incoordination on finger-nose testing and heel-knee-shin testing on the left.

What artery is most likely affected?

A

G. L vertebral

Atherosclerotic disease leads to an increased risk of vertebral artery occlusion leading to a posterior circulation stroke (cerebral infarction). The brainstem, cerebellum, and occipital lobes are commonly affected. Patients typically present with vestibulocerebellar signs (ataxia, dysmetria, dizziness, imbalance, vertigo, vomiting, nystagmus), ipsilateral cranial nerve dysfunction (dysphagia, dysarthria, vertical or horizontal gaze palsies), contralateral hemiparesis (corticospinal tract damage), contralateral impairment in pain and temperature sensation (spinothalamic tract damage), or potential contralateral homonymous hemianopsia with macular sparing (occipital lobe involvement).

In posterior circulation strokes affecting the lateral pons, Horner syndrome may occur, which presents with ipsilateral ptosis, miosis (pupillary constriction), and ipsilateral facial anhidrosis.

If no hemorrhage is demonstrated on non-contrast CT scan of the head, acute management of posterior circulation strokes commonly involves tissue plasminogen activator therapy or thrombectomy.

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11
Q

Anterior spinal artery occlusion presenting symptoms

A

bilateral loss of pain and temperature sensation and motor function below the level of the lesion, along with autonomic dysfunction.

The anterior spinal artery supplies the bilateral corticospinal, spinothalamic, and autonomic tracts.

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12
Q

basilar artery occlusion presenting symptoms

A

The basilar artery is supplied by the vertebral arteries. Basilar artery occlusion commonly presents with acute, severe, bilateral corticospinal and corticobulbar dysfunction, leading to locked-in syndrome.

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13
Q

occlusion of anterior cerebral artery (ACA) presenting symptoms

A

contralateral hemiparesis and sensory deficit of the lower extremities.

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14
Q

What artery is occluded?
R homonymous hemianopia w/ macular sparing and Gerstmann syndrome (agraphia, acalculia, finger agnosia, and left-right disorientation).

A

Left posterior cerebral artery (PCA)

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15
Q

ipsilateral sensory loss of proprioception, fine touch, and vibration below the level of the lesion.

A

posterior spinal artery
occlusion

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16
Q

MLD: Patient presenting post-viral infection w/ acute vertigo, nausea, vomiting, nystagmus, and gait instability.

A

Vestibular neuronitis.
Patients do not commonly present with hearing loss unless there is concomitant involvement of the auditory portion of cranial nerve VIII, which is referred to as labyrinthitis.

Vestibular neuronitis is typically self-limited, though a glucocorticoid taper may hasten recovery, and antiemetics and vertigo medications may reduce the severity of symptoms.

17
Q

episodic vertigo, hearing loss, and tinnitus

A

Meniere disease
pressure accumulation in the endolymph of the inner ear

18
Q

what is a more significant risk factor for ALZHEIMER’S DEMENTIA: family history or advancing age?

A

Dementia, Alzheimer type, is the most prevalent dementia, presenting with progressive cognitive decline across several domains. Advancing age is the most significant risk factor for AD.

Other major risk factors include a family history of AD, hypertension, dyslipidemia, cerebrovascular disease, atherosclerosis, and type II diabetes. Down syndrome has been shown to be associated with early- onset AD. Physical activity and management of cardiovascular risk factors have been shown to reduce the risk of AD. Treatment includes cholinesterase inhibitors, which may slow the rate of cognitive decline but do not cure AD.

19
Q

How do you diagnose botulism?

A

Botulism is an acute disease of the neuromuscular junction caused by exposure to the C. botulinum toxin. It presents with rapidly progressive, symmetric hypotonia and hyporeflexia that begins with the cranial nerves, manifesting as ptosis, sluggish pupils, and a diminished gag reflex, and descends to the lower extremities, as well as causes
constipation, poor feeding, and respiratory failure. The diagnosis is supported by a characteristic low amplitude response on repetitive nerve stimulation studies that improves with repeated stimulation.

20
Q

Constellation of findings for NF2?
Annual routine surveillance for NF2 includes what imaging?

A

Neurofibromatosis type 2 is characterized by a constellation of findings: bilateral acoustic schwannomas, cataracts, meningiomas, and ependymomas. Annual brain MRI is indicated as routine surveillance for patients with NF2 in order to monitor for the development of new tumors and growth of existing tumors.

21
Q

Prophylactic treatment for migraines?

A

For patients with disabling or frequent migraines, prophylactic treatment to reduce the frequency of migraine headaches is recommended and includes β- adrenergic blocking drugs, antidepressants, and anticonvulsants.

22
Q

In an otherwise healthy patient with HOCM, what class of medication would be protective against further complications and why?

A

Beta blockers (metoprolol) are useful to slow pulse rate (allowing for more filling time of L ventricle) and reduce likelihood of extopic beats.

HOCM results in hypertrophy of myocytes leading to a focal obstruction in the left ventricular outflow tract. It classically presents with syncope or sudden cardiac death, and is treated with β-adrenergic blockers, placement of implantable cardioverter-defibrillators, or cardiac surgery.

23
Q

Do ACE inhibitors affect preload or afterload?

A

Afterload

24
Q

Jugular venous distention that increases w/ inspiration is called what?
What diagnosis is it suggestive of?

A

Kussmaul sign, suggestive of constrictive pericarditis

Kussmaul sign indicates impaired right ventricular filling. Causes include constrictive pericardial disease, restrictive cardiomyopathy, pericardial effusion, large pulmonary embolism, tricuspid stenosis, and severe right heart failure.

25
Q

MOST LIKELY DIAGNOSIS: Old person w/ 3-month history of swelling and discoloration of his right leg that is mildly uncomfortable but not painful. History of DVT 9 months ago after knee replacement, INR was 2-3 during this period. He also has hyperlipidemia treated w/ atorvastatin.

On exam, vitals are wnl. The right lower extremity shows reddish-brown hyperpigmentation below the knee; there is edema and tenderness to palpation below the knee. There are well-healed arthroscopic scars over the knee. Distal pulses are intact. Venous duplex ultrasonography shows no abnormalities.

A

postphlebitic syndrome // post-thrombotic syndrome

Postphlebitic, or post-thrombotic, syndrome is a condition characterized by chronic venous insufficiency that can develop after deep vein thrombosis (DVT). Obstruction of venous flow leads to venous hypertension, inflammation, and vein wall remodeling, which can result in valvular incompetence and chronic venous reflux. Symptoms and signs include edema, skin pigmentation changes, pain, vein dilation, and venous ulcer formation. These typically develop weeks to months following a DVT and may be intermittent or progressive. Age, obesity, recurrent DVT, proximal thrombosis, delayed initiation of antithrombotic therapy, and inadequate treatment of the thrombus are risk factors for development and severity of post- thrombotic syndrome. Prevention of DVT with thromboprophylaxis, along with early diagnosis and treatment of DVTs lower the risk.

26
Q

describe classic presentation of superficial phlebitis

A

Superficial phlebitis is typically painful and associated with erythema, tenderness, and a palpable, thickened cord along the path of the affected vein.
It is typically self-limited, though may recur in associated inflammatory conditions, such as Buerger disease.

27
Q

MLD: Patient w/ history of recurrent nosebleeds, a GI bleed, and telangiectasia present on tongue and oral mucosa. Has first-degree relative w/ bleeding problems as well. Hematologic studies include a normal PT, PTT, bleeding time, and blood count.

A

Hereditary hemorrhagic telangiectasia (HHT)

Curacao criteria, which include the presence of recurrent bleeding, the presence of telangiectasias in typical locations (mucosal surfaces), a demonstrated visceral AVM, and the presence of a first-degree relative with HHT.
Treatment includes avoidance of blood thinning and antiplatelet agents, supportive care for minor bleeding, iron supplementation if anemia results, and surgical management of larger, complicated, or ruptured AVMs.

28
Q

Next best step in management for a 42 yo M here for wellness visit w/ no family history of CAD, nonsmoker, not obese. Normal BP and normal lipid studies (total cholesterol 190, HDL 40, triglyceride 150)

A

most asymptomatic men over the age of 35 and women over the age of 40 to 45 should be screened for hyperlipidemia. In those without other risk factors such as smoking, hypertension, or a family history of early myocardial infarction and normal cholesterol concentrations, repeat screening should be completed every 3 to 5 years.

this patient’s ASCVD risk is 1/6-3.3%. A risk less than 5% does not require intervention. A risk over 7.5% meet criteria for a statin. Between 5%-7.5% shared decision making.

(for reference, if this patient had the same normal labs and bp but was a smoker and had diabetes, he’d be 9-10.4% risk)

29
Q

A patient presents w/ pulse of 210/min but otherwise normal vital signs. Exam is normal. ECG showed regular, narrow complex tachycardia. Most likely diagnosis? Next best step?

A

stable supraventricular tachycardia should be acutely managed with vagal maneuvers and intravenous adenosine in an attempt to terminate or slow the arrhythmia, followed by AV-nodal blocking agents such as β- adrenergic blockers or calcium channel blockers, if refractory.

If hemodynamic instability is present (AMS, hypotension, angina, respiratory distress), the patient should undergo immediate electrical cardioversion.

30
Q

MLD: wide QRS complex tachycardia w/o identifiable P waves and presented after a syncopal episode with otherwise normal vitals, labs, and physical exam.

A

sustained Ventricular tachycardia (VT)

abnormal electrical focus or a re-entry circuit causes rapid contraction of the ventricles.
Risk factors include underlying structural heart disease, history of coronary artery disease, or myocardial infarction.
-Non-sustained VT lasts for less than 30 seconds
-sustained VT persists longer than 30 seconds and presents with varying symptoms such as palpitations and syncope.

31
Q

treatment for sustained stable VT

A

Class I or III antiarrhythmics (eg, lidocaine, amiodarone) are the frequent first-line therapy for stable, sustained VT.

32
Q

treatment for unstable sustained VT

A

Synchronized cardioversion may be necessary in cases of unstable, sustained VT

33
Q

treatment for pulseless VT

A

defibrillation is required for pulseless VT.

34
Q

what’s the arrhythmia?
irregular, narrow-complex tachyarrhythmia lacking P-waves

A

atrial fibrillation with rapid ventricular response

Atrial fibrillation with rapid ventricular response (heart rate >100 beats/minute) can result in reduced stroke volume and decreased cardiac output leading to symptomatic heart failure, and potentially hypotension and hemodynamic instability in severe cases.In the setting of a patient presenting with hemodynamic instability, the most appropriate initial treatment is synchronized cardioversion to quickly correct the arrhythmia and restore adequate cardiac output

35
Q

What medications can be used as rate control for stable Afib w/ RVR? Rhythm control?

A

-diltiazem (Ca Channel Blocker) or labetalol (B blocker) for rate control
-amiodarone (group III antiarrhythmic) for rhythm control, second line d/t side effects

36
Q
A